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Physico-mechanical and biological evaluation of heparin/VEGF-loaded electrospun polycaprolactone/decellularized rat aorta extracellular matrix for small-diameter vascular grafts

Authors
Cuenca, John PatrickKang, Hoe-JinAl Fahad, Md. AbdullahPark, MyeongkiChoi, MinjiLee, Hyun-YongLee, Byong-Taek
Issue Date
Aug-2022
Publisher
Taylor & Francis
Keywords
polycaprolactone; decellularized rat aorta matrix; vascular endothelial growth factor; Electrospinning; Decellularization; Small-diameter vascular grafts
Citation
Journal of Biomaterials Science, Polymer Edition, v.33, no.13, pp 1664 - 1684
Pages
21
Journal Title
Journal of Biomaterials Science, Polymer Edition
Volume
33
Number
13
Start Page
1664
End Page
1684
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/21400
DOI
10.1080/09205063.2022.2069398
ISSN
0920-5063
1568-5624
Abstract
Although the continuous development of small-diameter vascular grafts (SDVGs) (D < 5 mm) continues, most vascular grafts are made from synthetic polymers, which lead to serious complications from arteriosclerosis, thrombosis, and vascular ischemia. Here, to address these shortcomings, we combine synthetic polymers with natural decellularized small-diameter vessels and loaded with growth factor. We fabricated vascular grafts by electrospinning polycaprolactone (PCL) to decellularized rat aorta matrix (ECM) followed by heparin and vascular endothelial growth factor (VEGF) loading. In- vitro studies showed that PCL/ECM/VEGF vascular grafts, showed excellent hemocompatibility and biocompatibility properties. The vascular grafts implanted into the rat aorta revealed that the PCL/ECM/VEGF grafts promotes endothelial cells and smooth-muscle cells infiltration with a rate of FLK-1, ICAM1, and a-SMA distribution higher than that of the PCL and PCL/ECM vascular grafts at 2 weeks and 4 weeks after implantation. The PCL/ECM/VEGF vascular graft should be considered for potential small-diameter vascular grafts in clinical fields.
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